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    NDC 70518-2737-02 Losartan Potassium and Hydrochlorothiazide 25; 100 mg/1; mg/1 Details

    Losartan Potassium and Hydrochlorothiazide 25; 100 mg/1; mg/1

    Losartan Potassium and Hydrochlorothiazide is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM.

    Product Information

    NDC 70518-2737
    Product ID 70518-2737_0c510c12-bd17-a757-e063-6294a90a53c8
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Losartan Potassium and Hydrochlorothiazide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Losartan Potassium and Hydrochlorothiazide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25; 100
    Active Ingredient Units mg/1; mg/1
    Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091629
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2737-02 (70518273702)

    NDC Package Code 70518-2737-2
    Billing NDC 70518273702
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2737-2)
    Marketing Start Date 2023-12-06
    NDC Exclude Flag N
    Pricing Information N/A